← Back to catalogue

Enteral

FDA UDI

Class II (US FDA UDI)

by Gbuk Enteral Limited

Identity

Trade Name
Enteral FDA UDI
Generic Name
ENFit-formatted protective cap FDA UDI
Device Name
Enteral, Syringe Accessories, ENFit® Male Syringe Cap, Single Use 10/blister FDA UDI
Model / Reference
ECISO-10 FDA UDI
Description
Enteral, Syringe Accessories, ENFit® Male Syringe Cap, Single Use 10/blister FDA UDI

Identifiers

Catalog Number
ECISO-10 FDA UDI
Primary DI / UDI-DI
05060460848258 FDA UDI
FDA Product Code
PNR FDA UDI
GMDN Term
ENFit-formatted protective cap FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: ENFit-formatted protective cap

Enteral by Gbuk Enteral Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENFit-formatted protective cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 0ed53b80-1e2a-4093-86da-f7bdd6e282f8 34 fields · synced Jun 1, 2026